过电位
硫黄
氧气
电催化剂
氢
离解(化学)
拉曼光谱
化学
无机化学
吸收光谱法
尖晶石
材料科学
物理化学
电化学
电极
物理
光学
冶金
量子力学
有机化学
作者
Jing Jin,Jie Yin,Hongbo Liu,Bolong Huang,Yang Hu,Hong Zhang,Mingzi Sun,Yong Peng,Pinxian Xi,Chun‐Hua Yan
标识
DOI:10.1002/ange.202104055
摘要
Abstract The hydrogen evolution reaction (HER) usually has sluggish kinetics in alkaline solution due to the difficulty in forming binding protons. Herein we report an electrocatalyst in which sulfur atoms are doping in the oxygen vacancies (V O ) of inverse spinel NiFe 2 O 4 (S‐NiFe 2 O 4 ) to create active sites with enhanced electron transfer capability. This electrocatalyst has an ultralow overpotential of 61 mV at the current density of 10 mA cm −2 and long‐term stability of 60 h at 1.0 Acm −2 in 1.0 M KOH media. In situ Raman spectroscopy revealed that S sites adsorb hydrogen adatom (H*) and in situ form S‐H*, which favor the production of hydrogen and boosts HER in alkaline solution. DFT calculations further verified that S introduction lowered the energy barrier of H 2 O dissociation. Both experimental and theoretical investigations confirmed S atoms are active sites of the S‐NiFe 2 O 4 .
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